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Volume 4, Issue 6(Suppl)

J Infect Dis Ther

ISSN: 2332-0877 JIDT, an open access journal

Page 65

Influenza 2016

September 12-13, 2016

conferenceseries

.com

Influenza

September 12-13, 2016 Berlin, Germany

2

nd

International Conference on

J Infect Dis Ther 2016, 4:6(Suppl)

http://dx.doi.org/10.4172/2332-0877.C1.015

Molecular analysis of influenza A/H3N2 and A/H1N1pdm viruses circulating in the Democratic Republic

of Congo, 2014

Edith Nkwembe

1

, Roxana Cintron

2, 3

, Wendy Sessions

2

, Hugo Kavunga

1

, Pelagie Babakazo

3

, Leonie Manya

4

and

Jean Jacques Muyembe

1

1

Institut National de recherches Biomédicales, DR Congo

2

CDC Atlanta, USA

3

Battelle Memorial Institute, USA

4

Ecole de Santé Publique de l’UNIKIN, DR Congo

5

Direction de la Lutte contre la Maladie, Senegal

6

Centers for Disease Control and Prevention, DR Congo

Introduction & Aim

: Influenza is a common human respiratory infection and a cause of high morbidity and mortality. However,

not much is known about influenza viruses circulating in Democratic Republic of Congo (DRC). This study aimed to characterize

genetically and antigenically those strains affecting patients in this particular country.

Methods

: Nasal, throat and nasopharyngeal swabs from patients presenting with severe acute respiratory infections (SARI) or

influenza-like-illness (ILI) were collected from August to December, 2014 in various surveillance sites selected in DRC and delivered

to the National Institute of Biomedical Research (INRB) using the viral transport medium for molecular work. Viral RNA extraction

and amplification by reverse transcription polymerase chain reaction (RT-PCR) were done and positive influenza samples with a

Cycle threshold (Ct<30) were sent to the World Health Organization (WHO) Collaborating Center for Surveillance, Epidemiology

and Control of Influenza at the US Centers for Disease Control and Prevention (CDC) in Atlanta for further genetic and antigenic

characterization.

Results

: A total of 32 samples were tested at INRB and were found to be positive to influenza A with Ct<30. These samples were

shipped to the US CDC in Atlanta for further sub-typing: 26 samples were influenza A (H3N2), 2 were influenza A (H1N1) pdm09,

two samples were negative for influenza by RT-PCR and two samples contained insufficient volume for testing. The majority of

influenza A (H3N2) viruses tested from DRC was antigenically related to the A/Switzerland/9715293/2013 vaccine virus, while two

influenza A (H1N1) pdm09 virus isolates were antigenically characterized as A/California/07/2009-like. All A (H3N2) and A (H1N1)

pdm09 virus isolates characterized in this study from DRC were sensitive to oseltamivir and zanamivir.

Conclusion

: Two genetically distinct influenza subtypes, A (H3N2) and A (H1N1) pdm09, were found to be circulating in the DRC

during the study period. Based on these results, effective measures against influenza should be advised, including prevention of

infection by either vaccination or administration of antiviral drugs prophylactically or therapeutically.

edithnkwembe1@gmail.com